ATP synthase, H+ transporting, mitochondrial Fo complex subunit C3 (subunit 9)
OMIM: 602736, Gene2Phenotype
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ATP5G3 in Mitochondrial disorder with complex V deficiency
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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ATP5G3 in Likely inborn error of metabolism - targeted testing not possible
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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ATP5G3 in Possible mitochondrial disorder - nuclear genes
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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ATP5G3 in Mitochondrial disorders
Level 3: Mitochondrial
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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ATP5G3 in Childhood onset dystonia, chorea or related movement disorder
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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